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Yamaroku Shoyu Co., Ltd

FDA import alert and refusal historyShozu-Gun, JapanFEI 3009674466

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Example subjectYamaroku Shoyu Co., Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Yamaroku Shoyu Co., Ltd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on December 17, 2024, was classified VAI (Voluntary Action Indicated).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Yamaroku Shoyu Co., Ltd

2 records, newest first. Each line links to the FDA page it came from.

2024

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source
  2. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about Yamaroku Shoyu Co., Ltd

Is Yamaroku Shoyu Co., Ltd on an FDA import alert?
No listing for Yamaroku Shoyu Co., Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
Has FDA refused shipments from Yamaroku Shoyu Co., Ltd?
No FDA import refusals for Yamaroku Shoyu Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Yamaroku Shoyu Co., Ltd last inspected by FDA?
FDA's most recent inspection of Yamaroku Shoyu Co., Ltd with a final classification is dated December 17, 2024 and was classified VAI (Voluntary Action Indicated).
What is Yamaroku Shoyu Co., Ltd's FEI number?
Yamaroku Shoyu Co., Ltd's FDA Establishment Identifier (FEI) is 3009674466.

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Example subjectYamaroku Shoyu Co., Lt added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.